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5-hydroxypomalidomide

Base Information
  • Chemical Name:5-hydroxypomalidomide
  • CAS No.:1547162-41-3
  • Molecular Formula:C13H11N3O5
  • Molecular Weight:289.247
  • Hs Code.:
5-hydroxypomalidomide

Synonyms:

Suppliers and Price of 5-hydroxypomalidomide
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 4-Amino-2-(2,6-dioxo-3-piperidinyl)-5-hydroxy-1H-isoindole-1,3(2H)-dione
  • 100mg
  • $ 1540.00
  • TRC
  • 4-Amino-2-(2,6-dioxo-3-piperidinyl)-5-hydroxy-1H-isoindole-1,3(2H)-dione
  • 10mg
  • $ 195.00
Total 5 raw suppliers
Chemical Property of 5-hydroxypomalidomide
Chemical Property:
  • Boiling Point:633.0±55.0 °C(Predicted) 
  • Density:1.677±0.06 g/cm3(Predicted) 
Purity/Quality:

98% *data from raw suppliers

4-Amino-2-(2,6-dioxo-3-piperidinyl)-5-hydroxy-1H-isoindole-1,3(2H)-dione *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses 4-Amino-2-(2,6-dioxo-3-piperidinyl)-5-hydroxy-1H-isoindole-1,3(2H)-dione is an impurity of Pomalidomide (P688200). Pomalidomide is a thalidomide derivative, a potent inhibitor of TNF-α production. It is an antiinflammatory and antitumor agent used in the treatment of multiple myeloma.
Technology Process of 5-hydroxypomalidomide

There total 11 articles about 5-hydroxypomalidomide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
3-aminopiperidine-2,6-dione hydrochloric acid salt; With triethylamine; at 20 ℃; for 4h;
3-amino-4-hydroxyphthalic acid; With acetic acid; at 120 ℃; for 2.33333h;
Guidance literature:
Multi-step reaction with 4 steps
1.1: sulfuric acid; nitric acid / 2 h / 20 °C / Cooling with ice
2.1: palladium on activated charcoal; hydrogen / methanol / 20 °C
3.1: sodium hydroxide; water / ethanol / 70 °C
4.1: triethylamine / 4 h / 20 °C
4.2: 2.33 h / 120 °C
With sulfuric acid; palladium on activated charcoal; water; hydrogen; nitric acid; triethylamine; sodium hydroxide; In methanol; ethanol;
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